FDA Investigator Sondra R Davis
Sondra R Davis has conducted inspections on 60 sites in 1 countries as of 10 Jul 2024. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
60
Last Inspection Date:
10 Jul 2024
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America
FDA Investigators that have inspected at least one site in common with Sondra R Davis:
Aaron J Crawford,
Alex G Kalugin,
Aliza Chalapong Asawesna,
Alphonso A Haupt, III,
Amanda N Schaupp,
Andrea Ab Bautista,
Andrew B Slarve,
Andrew E Kay,
Andrew Tadros,
Arthur G Hurst,
Breena L D'ambrogi,
Brenda C Hamilton,
Chloe Anne Leong,
Christopher J Lee,
Christopher S Keating,
Clint R Van Blaricom,
Danielle Lyke,
David A Lum,
Dawn P Hall,
Deborah K Richardson,
Dena L Jacobs,
Devon Jenkins,
Devon M Shoop,
Diana M Guidry,
Diana M Raman,
Donzel R Lee,
Earl Echon,
Efrain E Meneses,
Elaine S Chow,
Elenita Yibarra Pratt,
Emil P Wang, JD,
Eric J Cross,
Estefania Fernandez,
Fidel Carrillo,
Frank P Bianco,
Frans E Mercado,
Gabriel E Muniz,
Gina Eng,
Helen J Hamaoka,
Ingrid A Zambrana,
Ismael Garibay,
James C Yee,
Jamie L Port,
Jane G Choi,
Janice Wai,
Jason D Tenney,
Jennifer Crumb,
Jennifer S King,
Jeremy R Read,
Joan T Briones,
Joanne M Fukuda,
John A Liu,
Joseph M Willems,
Justin A Hefferman,
Karen J Bak,
Katherine D Cogburn Perez,
Kimberly Cdelk Brooks,
Laura D Cain,
Lauren E Ciurca,
LCDR Audra J Lenhart,
Lisa H Nakagawa,
Lisa Shin,
Lorenzo F Edwards,
LT Mark A Chen, MPH,
Macropolk,
Mark E Baldwin,
Mcgrewp,
Michelle L Tripp,
Misty L Treece,
Myckie M Jacobsen,
Neal D Singletary, PhD,
Nicolas C Tolosa, III,
Niketa Patel,
Patrick J Legler,
Phung,
Randy L Elsberry,
Renisha M Garnes,
Samuel A Hamblin,
Sara M Richardson,
Savannah E Samp,
Sean P Desbrow,
Sharon L Shane,
Shelton L Stribling,
Sheri L Stephenson,
Siobhan A Gallagher,
Steven L Strom,
Steven M Galvez,
Sundy V Sedwick,
Thomas W Gordon,
Tuan D Tran,
Valerie L Whipp,
Wayne S Fortenberry,
William J Foust,
Young Kim
Sondra R Davis's Documents
| Publish Date | Document Type | Title |
|---|---|---|
| February, 2019 | FDA 483 | Vita-Pakt Citrus Products Co. - Form 483, 2019-02-08 |
| February, 2019 | EIR | Vita-Pakt Citrus Products Co. - EIR, 2019-03-19 |
Experience Redica Systems’ NEW investigator profiles and dashboards
Redica Systems customers get access to over 1,400 FDA Investigator profiles, containing powerful analysis like:
- Total inspections conducted
- 483 rate
- OAI rate
- Warning Letter rate
- Inspections by Industry, Scope, and Inspection Reason
- And much more
Investigator Profiles are not sold as on-demand documents. If you’d like to see one, fill out the form below to connect with our Sales Team and get it in your inbox as little as 24 hours.
Talk to sales to access our investigator profiles
Loading...
Investigator Profiles Are Just the Tip of the Iceberg
Becoming a Redica Systems customer not only provides you with unlimited access to profiles similar to the one above for every current and former FDA Investigator, but also grants you access to:
Inspection Intelligence
- Pre-Approval Inspection (PAI) trends
- The ability to filter nearly any FDA enforcement action by GxP labels like GMP, GCP, etc.
- Latest 483s: see what the trends are across all FDA Investigators
- CFR Heatmap: Citations aggregated by Subpart by Year
Vendor Intelligence
- Full inspection histories for your vendors down to the specific site level
- All of the functionality mentioned above but isolated to just your vendors
Regulatory Intelligence
- Zero in on the trends for a specific agency/regulator (ex. FDA, MHRA, EMA, Health Canada)
- All the latest "Signals" from agencies around the world, segmented by Country, Type (ex. Guidance, Decree...), Category (ex. Rules/Regulations/Guidance, News, Reports...), Theme (ex. Cell and Gene Therapy, AI...), and more